5254-94-4 Usage
Class
Isothiochromenone
A group of compounds known for their diverse biological and pharmacological activities.
Biological and pharmacological activities
Exhibits a range of effects on living organisms and their physiological functions.
Potential use as an anti-inflammatory agent
May help reduce inflammation in the body, which can be beneficial in treating various inflammatory conditions.
Potential use as an anticancer agent
May help prevent or treat cancer by inhibiting the growth and spread of cancer cells.
Modulation of cell signaling pathways
May influence the way cells communicate with each other, which can have various effects on cellular processes.
Inhibition of certain enzymes
May interfere with the activity of specific enzymes, potentially leading to therapeutic effects.
Antioxidant potential
May help protect cells from damage caused by free radicals and oxidative stress.
Induction of apoptosis in cancer cells
May cause cancer cells to undergo programmed cell death, which can be beneficial in treating cancer.
Therapeutic potential
Shows promise as a potential treatment for various medical conditions, including inflammation, cancer, and other diseases related to cellular processes and enzyme activity.
Check Digit Verification of cas no
The CAS Registry Mumber 5254-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5254-94:
(6*5)+(5*2)+(4*5)+(3*4)+(2*9)+(1*4)=94
94 % 10 = 4
So 5254-94-4 is a valid CAS Registry Number.
5254-94-4Relevant articles and documents
Synthesis of Cyclic α-Diazo-β-keto Sulfoxides in Batch and Continuous Flow
McCaw, Patrick G.,Buckley, Naomi M.,Eccles, Kevin S.,Lawrence, Simon E.,Maguire, Anita R.,Collins, Stuart G.
, p. 3666 - 3679 (2017/04/11)
Diazo transfer to β-keto sulfoxides to form stable isolable α-diazo-β-keto sulfoxides has been achieved for the first time. Both monocyclic and benzofused ketone derived β-keto sulfoxides were successfully explored as substrates for diazo transfer. Use of continuous flow leads to isolation of the desired compounds in enhanced yields relative to standard batch conditions, with short reaction times, increased safety profile, and potential to scale up.
